首页> 外文期刊>International medical journal: IMJ >Pre-Treatment with Reserpine Does Not Shorten the Duration of N-Methyl-N'-Nitro-N-Nitrosoguanidine (MNNG)-Induced Stomach Adenocarcinoma in Female Sprague-Dawley Rats
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Pre-Treatment with Reserpine Does Not Shorten the Duration of N-Methyl-N'-Nitro-N-Nitrosoguanidine (MNNG)-Induced Stomach Adenocarcinoma in Female Sprague-Dawley Rats

机译:用血纯化的预处理不会缩短N-甲基-N'-硝基-N-硝基胍(MNNG)的持续时间(MNNG)诱导女性Sprague-Dawley大鼠的胃腺癌

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Background: N-methyl-N'-nitro-N-nitrosoguanidine (MNNG) is often used to induce adenocarcinoma in the stomach of rats; taking about 40 weeks to develop. It is however less effective in female rats and it is unknown if its effectiveness could be improved and its duration shortened by pre-treatment with reserpine, an agent used to induce peptic ulceration. Objective: This study therefore examined the effects of MNNG-induced tumorigenesis in female Sprague-Dawley rats pre-treated with a single dose of reserpine. Design/Materials and Methods: Forty-eight, 6-week old female rats were divided into six groups. Group A, normal control euthanized at day 0; Group B, euthanized 24 hours after reserpine treatment; Groups D and F were treated with reserpine and MNNG and then euthanized at 20 and 40 weeks respectively; Groups C and E were treated with reserpine and acted as age-matched controls for groups D and F respectively. A stat intraperitoneal injection of 20 mg/kg of reserpine was given followed by daily administration of MNNG at a dose of 10 mg/kg/day in drinking water. Body weight and water intake were measured weekly throughout the study, and the data were analysed using 2-way ANOVA. Following euthanization, their stomachs were collected for histo-pathological examination. Results: There was no difference in body weight and water intake between the two groups. Stomachs of rats exposed to reserpine and MNNG for 40 weeks showed no evidence of tumour formation. Conclusion: Pre-treatment with reserpine to induce acute ulceration in the stomach of Sprague-Dawley rats did not result in the development of MNNG-induced stomach adenocarcinoma.
机译:背景:N-甲基-N'-NITRO-NITROSOGUANIDINE(MNNG)通常用于在大鼠胃中诱导腺癌;大约需要40周才能发展。然而,在雌性大鼠中,如果可以改善其有效性,并且通过用血清序列预处理缩短其持续时间,则尚不清楚,用于诱导消化溃疡的药剂。目的:本研究研究了用单剂量的血红素预处理的雌性Sprague-Dawley大鼠中Mnng诱导的肿瘤发生的影响。设计/材料和方法:四十八,6周龄雌性大鼠分为六组。第一个,正常控制在第0天安乐死; B组,在Realpine治疗后24小时安乐死;将D和F组用Reserpine和Mnng治疗,然后分别在20和40周安乐死;将C组和e分析治疗,并分别作为组D和F组的年龄匹配对照。给出了腹膜内注射20mg / kg血萜的注射,然后在饮用水10mg / kg /天的剂量下每日施用Mnng。在整个研究中每周测量体重和水摄入量,使用双向ANOVA分析数据。在安乐死之后,收集了他们的胃,用于组织病理学检查。结果:两组体重和水摄入量没有差异。暴露于Realerpine和Mnng的大鼠胃40周显示没有肿瘤形成的证据。结论:用血清诱导Sprague-Dawley大鼠胃中急性溃疡的预处理并未导致Mnng诱导的胃腺癌的发育。

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